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  2. Ethylene - Wikipedia

    en.wikipedia.org/wiki/Ethylene

    Ethylene (IUPAC name: ethene) is a hydrocarbon which has the formula C 2 H 4 or H 2 C=CH 2.It is a colourless, flammable gas with a faint "sweet and musky" odour when pure. [7] It is the simplest alkene (a hydrocarbon with carbon–carbon double bonds).

  3. Lewis structure - Wikipedia

    en.wikipedia.org/wiki/Lewis_structure

    Lewis structure of a water molecule. Lewis structures – also called Lewis dot formulas, Lewis dot structures, electron dot structures, or Lewis electron dot structures (LEDs) – are diagrams that show the bonding between atoms of a molecule, as well as the lone pairs of electrons that may exist in the molecule.

  4. Ethylene (data page) - Wikipedia

    en.wikipedia.org/wiki/Ethylene_(data_page)

    Phase behavior Triple point: 104 K (−169 °C), 120 Pa Critical point: 282.5 K (9.4 °C), 50.6 bar Std enthalpy change of fusion, Δ fus H o +3.35 kJ/mol Std entropy change

  5. Electron counting - Wikipedia

    en.wikipedia.org/wiki/Electron_counting

    It is used for classifying compounds and for explaining or predicting their electronic structure and bonding. [1] Many rules in chemistry rely on electron-counting: Octet rule is used with Lewis structures for main group elements, especially the lighter ones such as carbon, nitrogen, and oxygen,

  6. Vinyl group - Wikipedia

    en.wikipedia.org/wiki/Vinyl_group

    Chemical structure of the vinyl functional group. In organic chemistry , a vinyl group (abbr. Vi ; [ 1 ] IUPAC name : ethenyl group [ 2 ] ) is a functional group with the formula −CH=CH 2 . It is the ethylene (IUPAC name: ethene) molecule ( H 2 C=CH 2 ) with one fewer hydrogen atom.

  7. Zeise's salt - Wikipedia

    en.wikipedia.org/wiki/Zeise's_salt

    Zeise's salt received a great deal of attention during the second half of the 19th century because chemists could not explain its molecular structure. This question remained unanswered until the determination of its X-ray crystal structure in the 20th century.

  8. Hückel method - Wikipedia

    en.wikipedia.org/wiki/Hückel_method

    Delocalization energy is defined as the difference in energy between that of the most stable localized Lewis structure and the energy of the molecule computed from Hückel theory orbital energies and occupancies. Since all energies are relative, we set = without loss of generality to simplify discussion. The energy of the localized structure is ...

  9. Dewar–Chatt–Duncanson model - Wikipedia

    en.wikipedia.org/wiki/Dewar–Chatt–Duncanson...

    Orbital interactions in a metal-ethylene complex. On the left, a filled pi-orbital on C 2 H 4 overlaps with an empty d-orbital on the metal. On the right, an empty pi-antibonding orbital on C 2 H 4 overlaps with a filled d-orbital on the metal